Literature DB >> 28106360

Federal Policy for the Protection of Human Subjects. Final rule.

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Abstract

The departments and agencies listed in this document announce revisions to modernize, strengthen, and make more effective the Federal Policy for the Protection of Human Subjects that was originally promulgated as a Common Rule in 1991. This final rule is intended to better protect human subjects involved in research, while facilitating valuable research and reducing burden, delay, and ambiguity for investigators. These revisions are an effort to modernize, simplify, and enhance the current system of oversight.

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Year:  2017        PMID: 28106360

Source DB:  PubMed          Journal:  Fed Regist        ISSN: 0097-6326


  76 in total

1.  Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.

Authors:  Stephanie A Kraft; Mildred K Cho; Katherine Gillespie; Meghan Halley; Nina Varsava; Kelly E Ormond; Harold S Luft; Benjamin S Wilfond; Sandra Soo-Jin Lee
Journal:  Am J Bioeth       Date:  2018-04       Impact factor: 11.229

2.  Reaping the Bounty of Publicly Available Clinical Trial Consent Forms.

Authors:  Holly Fernandez Lynch; Emily A Largent; Deborah A Zarin
Journal:  IRB       Date:  2017 Nov-Dec

3.  From in vivo to in vitro: How the Guatemala STD Experiments Transformed Bodies Into Biospecimens.

Authors:  Kayte Spector-Bagdady; Paul A Lombardo
Journal:  Milbank Q       Date:  2018-04-13       Impact factor: 4.911

4.  New requirements for clinical trial transparency provide new opportunities for informatics research.

Authors:  Betsy L Humphreys
Journal:  J Am Med Inform Assoc       Date:  2019-06-01       Impact factor: 4.497

5.  Patient-Consent Disconnects in Clinical Research.

Authors:  Neal W Dickert; JoAnne Brabson; Rodney J Hunter; Michele Riedford
Journal:  Patient       Date:  2018-12       Impact factor: 3.883

6.  Concern about Justifying the Release of Genomic Data as a Civil Right.

Authors:  Jennifer C Dreyfus; Mark E Sobel
Journal:  Am J Hum Genet       Date:  2018-07-05       Impact factor: 11.025

7.  The Emergency Medicine Specimen Bank: An Innovative Approach To Biobanking In Acute Care.

Authors:  Jessica L Saben; Shelby K Shelton; Andrew J Hopkinson; Brandon J Sonn; Eleanor B Mills; Makayla Welham; Megan Westmoreland; Richard Zane; Adit A Ginde; Kelly Bookman; Justin Oeth; Mark Chavez; Michael DeVivo; Alison Lakin; John Heldens; Laurie Blumberg Romero; Michael J Ames; Emily R Roberts; Matthew Taylor; Kristy Crooks; Stephen J Wicks; Kathleen C Barnes; Andrew A Monte
Journal:  Acad Emerg Med       Date:  2018-10-25       Impact factor: 3.451

8.  A Measure of Effectiveness Is Key to the Success of sIRB Policy.

Authors:  Holly A Taylor; Ann Margret Ervin
Journal:  Am J Bioeth       Date:  2017-07       Impact factor: 11.229

9.  Biospecimens, Research Consent, and Distinguishing Cell Line Research.

Authors:  Kayte Spector-Bagdady; Holly Fernandez Lynch; J Chad Brenner; Andrew G Shuman
Journal:  JAMA Oncol       Date:  2019-03-01       Impact factor: 31.777

Review 10.  "The Google of Healthcare": enabling the privatization of genetic bio/databanking.

Authors:  Kayte Spector-Bagdady
Journal:  Ann Epidemiol       Date:  2016-06-01       Impact factor: 3.797

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